Tethered molecular redox capacitors for nanoconfinement-assisted electrochemical signal amplification
Source abstract
Abstract
Nanostructured materials offer the potential to drive future developments and applications of electrochemical devices, but are underutilized because their nanoscale cavities can impose mass transfer limitations that constrain electrochemical signal generation. Here, we report a new signal-generating mechanism that employs a molecular redox capacitor to enable nanostructured electrodes to amplify electrochemical signals even without an enhanced reactant mass transfer. The surface-tethered molecular redox capacitor engages diffusible reactants and products in redox-cycling reactions with the electrode. Such redox-cycling reactions are facilitated by the nanostructure that increases the probabilities of both reactant-electrode and product-redox-capacitor encounters (i.e., the nanoconfinement effect), resulting in substantial signal amplification. Using redox-capacitor-tethered Au nanopillar electrodes, we demonstrate improved sensitivity for measuring pyocyanin (bacterial metabolite). This study paves a new way of using nanostructured materials in electrochemical applications by engineering the reaction pathway within the nanoscale cavities of the materials.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Conducting polymers and applications · Electrochemical Analysis and Applications · Analytical Chemistry and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Advanced Nano-Surface Department
Korea Institute of Materials Science (KIMS)
Changwon
South Korea
Institute for Bioscience and Biotechnology Research
University of Maryland
College Park
USA
Department of Chemistry
Pusan National University
Busan 46241
Funding
Korea Institute of Materials Science · Ministry of Trade, Industry and Energy · National Science Foundation
References (42)
Show source-provided references
1. Wongkaew · Chem. Rev. · 2019 · 119 · 12010.1021/acs.chemrev.8b00172 ↗
2. Chen · Chem. Soc. Rev. · 2013 · 42 · 542510.1039/c3cs35518g ↗
3. Zhu · Anal. Chem. · 2015 · 87 · 23010.1021/ac5039863 ↗
4. Zhou · Nano Today · 2018 · 20 · 3310.1016/j.nantod.2018.04.002 ↗
5. Trogadas · Angew. Chem., Int. Ed. · 2016 · 55 · 12210.1002/anie.201506394 ↗
6. Yu · Adv. Mater. · 2017 · 29 · 160456310.1002/adma.201604563 ↗
7. Waser · Adv. Mater. · 2009 · 21 · 263210.1002/adma.200900375 ↗
8. Park · Analyst · 2012 · 137 · 389110.1039/c2an35294j ↗
9. Seo · Curr. Opin. Electrochem. · 2019 · 13 · 4710.1016/j.coelec.2018.10.011 ↗
10. Xiao · Biotechnol. Adv. · 2016 · 34 · 23410.1016/j.biotechadv.2016.01.006 ↗
11. Snyder · J. Am. Chem. Soc. · 2012 · 134 · 863310.1021/ja3019498 ↗
12. Luo · ACS Nano · 2009 · 3 · 212110.1021/nn9003154 ↗
13. White · Anal. Chem. · 2005 · 77 · 214A10.1021/ac053391e ↗
14. Di Mundo · Plasma Processes Polym. · 2012 · 9 · 94710.1002/ppap.201200041 ↗
15. Lee · Sci. Rep. · 2018 · 8 · 1406310.1038/s41598-018-32378-2 ↗
16. Yun · Energy Environ. Sci. · 2015 · 8 · 93210.1039/C4EE01100G ↗
17. Park · Adv. Funct. Mater. · 2017 · 27 · 170337610.1002/adfm.201703376 ↗
18. Wang · Small · 2018 · 14 · 180162310.1002/smll.201801623 ↗
19. Hoogvliet · Anal. Chem. · 2000 · 72 · 201610.1021/ac991215y ↗
20. Kim · Anal. Chem. · 2013 · 85 · 210210.1021/ac302703y ↗
21. Bellin · Nat. Commun. · 2014 · 5 · 325610.1038/ncomms4256 ↗
22. Kim · Analyst · 2014 · 139 · 3210.1039/C3AN01632C ↗
23. Kashiwagi · J. Flow Chem. · 2012 · 3 · 1710.1556/JFC-D-12-00019 ↗
24. Sugumaran · Int. J. Mol. Sci. · 2016 · 17 · 157610.3390/ijms17091576 ↗
25. Bai · Electroanalysis · 2010 · 22 · 175010.1002/elan.200900538 ↗
26. Liu · Bioelectrochemistry · 2014 · 98 · 9410.1016/j.bioelechem.2014.03.012 ↗
27. Sanger · ACS Sens. · 2017 · 2 · 186910.1021/acssensors.7b00783 ↗
28. Szamocki · Angew. Chem., Int. Ed. · 2006 · 45 · 131710.1002/anie.200503292 ↗
29. Lau · Trends Mol. Med. · 2004 · 10 · 59910.1016/j.molmed.2004.10.002 ↗
30. Vincent · JAMA, J. Am. Med. Assoc. · 2009 · 302 · 232310.1001/jama.2009.1754 ↗
31. Fick Jr. · Chest · 1989 · 96 · 15810.1378/chest.96.1.158 ↗
32. Lister · Clin. Microbiol. Rev. · 2009 · 22 · 58210.1128/CMR.00040-09 ↗
33. Buzid · Sci. Rep. · 2016 · 6 · 3000110.1038/srep30001 ↗
34. Elliott · Anal. Chem. · 2017 · 89 · 628510.1021/acs.analchem.7b00876 ↗
35. Ciui · Anal. Chem. · 2018 · 90 · 776110.1021/acs.analchem.8b01915 ↗
36. Sismaet · Analyst · 2014 · 139 · 424110.1039/C4AN00756E ↗
37. Sismaet · Biosens. Bioelectron. · 2017 · 97 · 6510.1016/j.bios.2017.05.042 ↗
38. Burkitt · Electrochem. Commun. · 2017 · 78 · 4310.1016/j.elecom.2017.03.021 ↗
39. Alatraktchi · PLoS One · 2018 · 13 · e019415710.1371/journal.pone.0194157 ↗
40. Seviour · Chem. Commun. · 2015 · 51 · 378910.1039/C4CC08590F ↗
41. Alatraktchi · Nanomedicine · 2016 · 11 · 218510.2217/nnm-2016-0155 ↗
42. Hall · Toxins · 2016 · 8 · 23610.3390/toxins8080236 ↗